Anticoagulation in Post MI LV Thrombus Trial in Nepal

PHASE4RecruitingINTERVENTIONAL
Enrollment

196

Participants

Timeline

Start Date

June 19, 2023

Primary Completion Date

March 31, 2026

Study Completion Date

April 30, 2026

Conditions
Left Ventricular ThrombusMyocardial Infarction
Interventions
DRUG

Rivaroxaban

"Intervention Group:~The patients in the intervention group will be treated with Rivaroxaban 20 mg once daily with the evening meal in patients with a CrCl \>50 mL/min OR 15 mg in cases of moderate-to-severe renal impairment dose with the dosing of once daily with the evening meal in patients with a CrCl ≤50 mL/min. The patient in the intervention group will be requested for follow-up after 3 months of commencing the treatment or whenever the signs and symptoms of bleeding events are noted."

DRUG

Warfarin

"Control Group:~The patients in the control group will be treated with Warfarin. The dose will be started with 5 mg and will be titrated based on the International Normalized Ratio (INR) which will be targeted at the range of 2.0 to 3.0. The dual antiplatelet duration will be based on the latest guidelines. The patients will be asked for frequent INR monitoring on an OPD basis until the INR is within the therapeutic range, after which patients will be asked for monthly follow-up INR reports. The patients in the control group will not be treated with heparin or low molecular weight heparin before the INR is maintained in the therapeutic range."

Trial Locations (1)

Unknown

RECRUITING

Nepal Health Research Council, Kathmandu

All Listed Sponsors
lead

Shahid Gangalal National Heart Centre

OTHER